IRGM, immunity related GTPase M, 345611

N. diseases: 57; N. variants: 13
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1000113
rs1000113
0.925 0.040 5 150860514 intron variant C/T snv 0.13
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.840 1.000 5 2007 2015
dbSNP: rs11747270
rs11747270
0.790 0.240 5 150879305 intron variant A/G snv 0.21
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.820 0.667 3 2008 2020
dbSNP: rs11741861
rs11741861
0.925 0.040 5 150898347 intron variant A/G snv 8.8E-02
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.800 1.000 2 2012 2017
dbSNP: rs7714584
rs7714584
1.000 0.040 5 150890858 intron variant A/G snv 0.21
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.800 1.000 1 2010 2010
dbSNP: rs11741861
rs11741861
0.925 0.040 5 150898347 intron variant A/G snv 8.8E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.700 1.000 2 2015 2017
dbSNP: rs11741861
rs11741861
0.925 0.040 5 150898347 intron variant A/G snv 8.8E-02
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs11747270
rs11747270
0.790 0.240 5 150879305 intron variant A/G snv 0.21
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs11747270
rs11747270
0.790 0.240 5 150879305 intron variant A/G snv 0.21
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs11749391
rs11749391
0.827 0.120 5 150849504 intron variant T/C snv 0.21
CUI: C0033860
Disease: Psoriasis
Psoriasis
Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs11749391
rs11749391
0.827 0.120 5 150849504 intron variant T/C snv 0.21
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs11749391
rs11749391
0.827 0.120 5 150849504 intron variant T/C snv 0.21
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs11749391
rs11749391
0.827 0.120 5 150849504 intron variant T/C snv 0.21
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
Musculoskeletal Diseases 0.700 1.000 1 2016 2016
dbSNP: rs11749391
rs11749391
0.827 0.120 5 150849504 intron variant T/C snv 0.21
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs10065172
rs10065172
0.790 0.200 5 150848436 synonymous variant C/T snv 0.17 0.21
CUI: C2677079
Disease: Inflammatory Bowel Disease 19
Inflammatory Bowel Disease 19
Digestive System Diseases 0.700 0
dbSNP: rs4958847
rs4958847
0.807 0.120 5 150860025 intron variant G/A snv 0.25
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.080 0.875 8 2008 2020
dbSNP: rs10065172
rs10065172
0.790 0.200 5 150848436 synonymous variant C/T snv 0.17 0.21
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.070 0.857 7 2011 2014
dbSNP: rs10065172
rs10065172
0.790 0.200 5 150848436 synonymous variant C/T snv 0.17 0.21
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
Infections 0.040 0.750 4 2011 2017
dbSNP: rs4958847
rs4958847
0.807 0.120 5 150860025 intron variant G/A snv 0.25
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.030 0.667 3 2009 2013
dbSNP: rs72553867
rs72553867
0.925 0.080 5 150848404 missense variant C/A;T snv 4.9E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.030 1.000 3 2013 2019
dbSNP: rs1000113
rs1000113
0.925 0.040 5 150860514 intron variant C/T snv 0.13
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs10051924
rs10051924
1.000 0.040 5 150847077 5 prime UTR variant T/C snv 0.21
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
Infections 0.010 1.000 1 2016 2016
dbSNP: rs10065172
rs10065172
0.790 0.200 5 150848436 synonymous variant C/T snv 0.17 0.21
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs10065172
rs10065172
0.790 0.200 5 150848436 synonymous variant C/T snv 0.17 0.21
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary
Infections; Respiratory Tract Diseases 0.010 1.000 1 2017 2017
dbSNP: rs10065172
rs10065172
0.790 0.200 5 150848436 synonymous variant C/T snv 0.17 0.21
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
Musculoskeletal Diseases 0.010 < 0.001 1 2017 2017
dbSNP: rs10065172
rs10065172
0.790 0.200 5 150848436 synonymous variant C/T snv 0.17 0.21
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
Digestive System Diseases; Nutritional and Metabolic Diseases 0.010 1.000 1 2009 2009